A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068175



Internal ID21490759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24656213..24656937hg38UCSC Ensembl
chr10:24945142..24945866hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38725
hg19725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5599089
Supporting Variants
SamplesNA19238
Known GenesARHGAP21
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068175
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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